USV Private Limited, a leading pharmaceutical and healthcare company, has announced exciting career opportunities at its Daman manufacturing facility. The company invites applications from qualified and experienced pharmaceutical professionals for positions in QC Microbiology and QA Sterile/Injectables departments.

USV is a 63-year-old healthcare company with a presence in more than 65 countries and a strong position in the oral anti-diabetic segment. Candidates with relevant pharmaceutical qualifications and experience can apply for the latest vacancies.

Job Details – USV Private Limited Recruitment 2026

Company Name: USV Private Limited

Job Location: Daman, India

Industry: Pharmaceutical / Healthcare

Recruitment Type: Experienced Professionals

Application Mode: Email

1. QC Microbiology – Environmental Monitoring

Department: QC Microbiology

Section: Environmental Monitoring

Designation: Officer / Senior Officer / Executive

Experience Required: 2 to 8 Years

Educational Qualification: M.Sc. in Microbiology

Key Responsibilities:

• Perform environmental monitoring activities in classified manufacturing areas.
• Conduct viable and non-viable particle monitoring.
• Perform microbial air sampling and surface monitoring.
• Monitor personnel hygiene and microbiological contamination.
• Maintain environmental monitoring records and documentation.
• Investigate microbial excursions and support corrective and preventive actions (CAPA).
• Ensure compliance with GMP and applicable regulatory requirements.

2. QA Sterile / Injectables – IPQA

Department: QA Sterile / Injectables

Section: IPQA (In-Process Quality Assurance)

Designation: Executive / Senior Executive / Assistant Manager

Experience Required: 6 to 12 Years

Educational Qualification: B.Pharm / M.Pharm / M.Sc.

Key Responsibilities:

• Perform in-process quality assurance activities in sterile and injectable manufacturing.
• Monitor aseptic manufacturing operations and cleanroom practices.
• Ensure compliance with cGMP and applicable regulatory guidelines.
• Review batch manufacturing and packaging records.
• Monitor line clearance and process compliance.
• Handle deviations, investigations, CAPA and change controls.
• Ensure proper documentation and compliance with quality standards.
• Support audits and regulatory inspections.

How to Apply for USV Recruitment 2026?

Interested and eligible candidates are requested to share their updated CV through email.

Email ID: Sanafatma.khan@usv.in

Job Location: Daman

Candidates should mention their relevant department and designation in the email subject line while submitting their updated resumes.

Important: Applicants should carefully check the required qualification and experience before applying.

5 Technical Frequently Asked Questions (FAQs)

Q1. What are the major activities involved in environmental monitoring in pharmaceutical manufacturing?

Environmental monitoring includes viable and non-viable particle monitoring, active air sampling, settle plate monitoring, surface monitoring and personnel monitoring to assess microbiological contamination in controlled manufacturing environments.

Q2. What is the difference between viable and non-viable particle monitoring?

Viable monitoring detects microorganisms such as bacteria and fungi present in the manufacturing environment, whereas non-viable monitoring measures airborne particulate matter without determining whether the particles are living organisms.

Q3. What is IPQA in sterile pharmaceutical manufacturing?

IPQA stands for In-Process Quality Assurance. It involves monitoring manufacturing activities, checking process compliance, performing line clearance, reviewing batch documentation and ensuring adherence to cGMP requirements throughout production.

Q4. What is the importance of aseptic process control in injectable manufacturing?

Aseptic process control helps prevent microbial contamination during sterile product manufacturing. It involves maintaining cleanroom conditions, personnel hygiene, equipment sterilization, environmental monitoring and validated aseptic practices.

Q5. What are deviation, CAPA and change control in pharmaceutical quality assurance?

• Deviation: An unexpected departure from an approved procedure, process or specification.
• CAPA: Corrective and Preventive Action taken to identify root causes, correct issues and prevent recurrence.
• Change Control: A formal system for evaluating, approving, implementing and documenting changes that may affect product quality.

Conclusion

USV Private Limited offers excellent career opportunities for experienced pharmaceutical professionals in QC Microbiology and QA Sterile/Injectables at its Daman facility. Candidates with M.Sc. Microbiology, B.Pharm, M.Pharm and relevant industry experience can apply for these positions.

Interested candidates should send their updated CV to Sanafatma.khan@usv.in and explore this opportunity to advance their careers in the pharmaceutical industry.